Testing Genotypic and Phenotypic Resistance in Human Immunodeficiency Virus Type 1 Isolates of Clade B and Other Clades from Children Failing Antiretroviral Therapy

Author:

Brindeiro Patrícia A.1,Brindeiro Rodrigo M.1,Mortensen Cláudio2,Hertogs Kurt3,De Vroey Veronique3,Rubini Norma P. M.4,Sion Fernando S.4,De Sá Carlos A. M.4,Machado Deisy M.5,Succi Regina C. M.5,Tanuri Amilcar1

Affiliation:

1. Laboratory of Molecular Virology, Department of Genetics, Federal University of Rio de Janeiro

2. Applied Biosystems

3. Tibotec-VIRCO NV, Mechelen, Belgium

4. Gaffrée & Guinle University Hospital, Rio de Janeiro

5. Federal University of São Paulo Medical School, São Paulo, Brazil

Abstract

ABSTRACT The emergence of resistance to antiretroviral drugs is a major obstacle to the successful treatment of human immunodeficiency virus type 1 (HIV-1)-infected patients. In this work, we correlate clinical and virological trends such as viral load (VL) and CD4 counts to genotypic and phenotypic antiretroviral (ARV) resistance profiles of HIV-1 isolates from the B and non-B subtypes found in vertically infected children failing ARV therapy. Plasma samples were collected from 52 vertically HIV-1-infected children failing different ARV therapies. Samples underwent HIV-1 pol sequencing and phenotyping and were clustered into subtypes by phylogenetic analysis. Clinical data from each patient were analyzed together with the resistance (genotypic and phenotypic) data obtained. Thirty-five samples were from subtype B, 10 samples were non-B (subtypes A, C, and F), and 7 were mosaic samples. There was no significant difference concerning treatment data between B and non-B clades. Prevalence of known drug resistance mutations revealed slightly significant differences among B and non-B subtypes: L10I, 21 and 64%, K20R, 13 and 43%, M36I, 34 and 100%, L63P, 76 and 36%, A71V/T, 24 and 0%, and V77I, 32 and 0%, respectively, in the protease (0.0001 ≤ P ≤ 0.0886), and D67N, 38 and 8%, K70R, 33 and 0%, R211K, 49 and 85%, and K219Q/E, 31 and 0%, respectively, in the reverse transcriptase (0.0256 ≤ P ≤ 0.0704). Significant differences were found only in secondary resistance mutations and did not reflect significant phenotypic variation between clade B and non-B.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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